TrialPal MoVi: An Intelligent Approach to Monitoring Visits in Clinical Trials

Say goodbye to inflexible systems and paperwork. Clinical Research Associates can create customized reports, monitor data, and personalize workflows with TrialPal MoVi's multilingual, user-friendly platform.

Schedule a Demo

Control Visit Monitoring
in One
Centralized Platform

ensayos clínicos desde un software centralizado

SDV records and safety data

Deviations from protocols

Scheduling and monitoring visitss

TrialPal MoVi is a secure and validated web-based system that complies with FDA regulation 21 CFR Part 11, designed to accelerate the visit monitoring process from scheduling to report approval, during a clinical trial.

Create, examine, and approve monitoring visit reports with ease while keeping complete control. Additionally,
TrialPal MoVi Simplifies:

Además, TrialPal MoVi simplifica:

Follow-Up Visit Monitoring Reports and Dashboards in One Place

Submission/approval deadlines for follow-up monitoring visit reports and the resulting reports can be viewed for detailed monitoring of the trial's status. This information can also be analyzed through customized dashboards, which allow the clinical trial's indicators and metrics to be viewed in real time for timely decision-making.

Reportes Dashboard

View direct statistics on the progress of each report. In addition to viewing available reports, you have direct access to reports pending completion or approval.

Visit

This module allows you to create and configure visits in the system. A customized report will be generated for each visit based on This module allows you to create and configure visits in the system. A customized report will be generated for each visit based on the clinical study's requirements. Two users, who will assume the roles of Manager and Reviewer, will be associated to complete the reports and have them reviewed in a single, continuous visit flow.

Document

This module allows you to view the templates that will be used for the various system information exports. It also includes a template preview to include the necessary information in the desired style.

Trascendent Data

Also known as the study database, it allows to view all significant events classified by type in a table format. These include action items, protocol deviations, safety information, SDV records, etc. It also has the option of exporting to Excel for better control.

Study Dashboard

Access dashboard panels with personalized metrics per study and get an overview of indicators like SAE reports SAE times, report type, and record dates of sponsor notifications in a graphic view. This functionality is a time-saving tool for CROs and enables them to spend less time on transcription and paper tasks, so they can focus on analytics and efficiency.

CRA (Clinical Research Associates)

In TrialPal MoVi, users with the CRA (Clinical Research Associates) role complete monitoring reports using a validation system that prevents certain formatting and typing errors. Additionally, users can save a report as a draft and continue it later without having to submit it for approval. They can also plan their monitoring activities and review study and research site information.

Project Managers (PMs)

Project Managers (PMs) can manage multiple sites, review reports, and manage study information; specific personnel can access information to support planning and monitoring activities (e.g., CTAs) and perform oversight activities (e.g., line managers, quality department).

Monitors

Within TrialPal MoVi, monitors and project managers certify that all processes are carried out in accordance with best practices by electronically signing reports.

Report Type

Depending on the study requirements, TrialPal MoVi offers the following report types:

Research site

Contract Research Organizations

Sponsors

Other Industry Solutions

Síganos